[CAS NO. 80286-36-8]  Balanophonin

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PRODUCTS SPECIFICATIONS [80286-36-8]

Catalog
HY-N10782
Brand
MCE
CAS
80286-36-8

DESCRIPTION [80286-36-8]

Overview

MDL-
Molecular Weight356.37
Molecular FormulaC20H20O6
SMILESOC[C@@H]1C2=CC(/C=C/C=O)=CC(OC)=C2O[C@H]1C3=CC(OC)=C(C=C3)O

For research use only. We do not sell to patients.

Summary

Balanophonin is an anti-inflammatory and anti-cancer agent. Balanophonin inhibits microglial activation and neurodegeneration via inhibiting activated microglia-induced apoptosis [1] .


IC50 & Target

COX-2

p38


In Vitro

Balanophonin (1-10 μM; 24 h) reduces Lipopolysaccharides (LPS; HY-D1056)-mediated TLR4 activation and NO production in BV2 cells [1] .
Balanophonin (1-10 μM; 6 h) reduces iNOS and COX2 protein expression and TNF-α and IL-1β production in LPS-induced microglial cells [1] .
Balanophonin (1-10 μM; 30 min) effectively inhibits MAPK activation [1] .
Balanophonin (1-10 μM; 24 h) inhibits neuronal cell death resulting from LPS-activated microglia by regulating cleaved caspase-3 and poly ADP ribose polymerase (PARP) cleavage in N2a cells [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis [1]

Cell Line: LPS-activated BV-2 cells
Concentration: 1, 5, and 10 μM
Incubation Time: 30 min for MAPKs, 6 h for iNOS and COX2 and 24 h for PGE2, TNF-α and IL-1β
Result: Downregulated TLR4. Reduced iNOS and COX2 expression. Significantly reduced the secretion of TNF-α and IL-1β. Decreased the phosphorylation of MAPKs such as pERK, pJNK, and p-p38.

Western Blot Analysis [1]

Cell Line: Neuroblastoma N2a cells
Concentration: 1, 5, and 10 μM
Incubation Time: 24 h
Result: Slightly increased Bcl-2. Inhibited caspase-3 activation and PARP cleavage.


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Storage

Please store the product under the recommended conditions in the Certificate of Analysis.